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Download fileInvestigation of the Capacity of Low Glass Transition Temperature Excipients to Minimize Amorphization of Sulfadimidine on Comilling
journal contribution
posted on 07.01.2013, 00:00 by Vincent Curtin, Youness Amharar, Yun Hu, Andrea Erxleben, Patrick McArdle, Vincent Caron, Lidia Tajber, Owen I. Corrigan, Anne Marie HealyThe coprocessing of active pharmaceutical ingredient
(API) with
an excipient which has a high glass transition temperature (Tg) is a recognized strategy to stabilize the
amorphous form of a drug. This work investigates whether coprocessing
a model API, sulfadimidine (SDM) with a series of low Tg excipients, prevents or reduces amorphization of the
crystalline drug. It was hypothesized that these excipients could
exert a Tg lowering effect, resulting
in composite Tg values lower than that
of the API alone and promote crystallization of the drug. Milled SDM
and comilled SDM with glutaric acid (GA), adipic acid (AA), succinic
acid (SA), and malic acid (MA) were characterized with respect to
their thermal, X-ray diffraction, spectroscopic, and vapor sorption
properties. SDM was predominantly amorphous when milled alone, with
an amorphous content of 82%. No amorphous content was detected by
dynamic vapor sorption (DVS) on comilling SDM with 50% w/w GA, and
amorphous content of the API was reduced by almost 30%, relative to
the API milled alone, on comilling with 50% w/w AA. In contrast, amorphization
of SDM was promoted on comilling with 50% w/w SA and MA, as indicated
by near-infrared (NIR) spectroscopy. Results indicated that the API
was completely amorphized in the SDM:MA comilled composite. The saturated
solubility of GA and AA in the amorphous API was estimated by thermal
methods. It was observed that the Tg of
the comelt quenched composites reached a minimum and leveled out at
this solubility concentration. Maximum crystallinity of API on comilling
was reached at excipient concentrations comparable to the saturated
concentration solubility of excipient in the API. Moreover, the closer
the Hildebrand solubility parameter of the excipient to the API, the
greater the inhibition of API amorphization on comilling. The results
reported here indicate that an excipient with a low Tg coupled with high solubility in the API can prevent
or reduce the generation of an amorphous phase on comilling.
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Keywords
Low Glass Transition Temperature ExcipientsComillingThe coprocessingexcipient concentrationsGANIRMaximum crystallinityMilled SDMvapor sorption propertiesmodel APIsolubility concentrationMATg excipientsMinimize AmorphizationDVSglass transition temperatureAPI amorphizationconcentration solubilityvapor sorptionSAHildebrand solubility parametercomelt quenched compositescomilling SDMAATg valuesmalic acidcomilled SDM